Senior Electronic Design Engineer

You will lead the design and development of mixed-signal electronic systems for next‑generation ophthalmic and imaging devices. This role requires deep technical ownership across the full product lifecycle — from concept through to design transfer — with a strong emphasis on EMC/ESD robustness and regulatory compliance.

You will play a critical role in delivering reliable, high-performance systems in a regulated medical environment.

• Proven track record delivering products from concept to production
• Hands‑on experience with EMC/ESD design and debugging
• Experience with high‑speed interfaces, sensors, or imaging systems
• Proficiency in schematic and PCB design tools (e.g., Altium or equivalent)
• Strong understanding of signal integrity, grounding, and power design
• Experience working in cross‑functional engineering teams
• Experience in medical devices or regulated environments
• Familiarity with IEC 60601, IEC 62304, ISO 13485
• Experience with ultrasound, imaging systems, or optical devices
• Exposure to pre‑compliance and certification testing (EMC, safety)
• Experience working with external design consultancies

• Design and develop mixed‑signal electronic systems (analog + digital) for medical devices
• Own schematic capture, PCB layout guidance, and bring‑up of complex boards
• Lead EMC/ESD design strategy, pre‑compliance testing, and issue resolution
• Support system integration across hardware, firmware, optics, and software
• Drive design for reliability, manufacturability, and testability (DFx)
• Contribute to risk management (ISO 14971) and safety requirements (IEC 60601)
• Support verification & validation, including environmental and lifecycle testing
• Work closely with external partners and suppliers on design and troubleshooting
• Contribute to design transfer into manufacturing, including documentation and test strategies
• Ensure designs pass EMC and safety testing with minimal rework
• Develop robust hardware that integrates cleanly into system architecture
• Strong contribution to programme delivery timelines
• Provide clear, high‑quality documentation supporting regulatory submissions